A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17355508



Internal ID22581177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:60766156..60767967hg38UCSC Ensembl
chr11:60533629..60535440hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg381812
hg191812
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5912592
Supporting Variants
Samples
Known GenesMS4A15
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17355508
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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